Variant report

Variant	nsv885863
Chromosome Location	chr6:44890760-45083966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:906)
CpG islands
(count:122)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:906 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45081891-45082077	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:44928633-44929024	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:45011822-45012263	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:45017618-45017640	K562	blood:	n/a	n/a
5	ARID3A	chr6:45025490-45025613	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:44942228-44942585	K562	blood:	n/a	n/a
7	ARID3A	chr6:44907927-44908749	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:44934203-44935340	K562	blood:	n/a	n/a
9	ARID3A	chr6:44900932-44900942	K562	blood:	n/a	n/a
10	ARID3A	chr6:44918920-44919276	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:45017086-45017200	HepG2	liver:	n/a	n/a
12	ATF1	chr6:45016978-45017291	K562	blood:	n/a	n/a
13	ATF1	chr6:44934477-44934865	K562	blood:	n/a	n/a
14	ATF1	chr6:45025523-45025589	K562	blood:	n/a	n/a
15	ATF1	chr6:44893099-44893531	K562	blood:	n/a	n/a
16	ATF2	chr6:44966734-44967257	GM12878	blood:	n/a	n/a
17	ATF2	chr6:44966735-44967151	GM12878	blood:	n/a	n/a
18	ATF3	chr6:44934407-44934925	K562	blood:	n/a	n/a
19	BACH1	chr6:44965357-44965412	K562	blood:	n/a	n/a
20	BATF	chr6:44966783-44967196	GM12878	blood:	n/a	n/a
21	BATF	chr6:44977286-44977716	GM12878	blood:	n/a	chr6:44977540-44977551
22	BATF	chr6:44966841-44967148	GM12878	blood:	n/a	n/a
23	BATF	chr6:44947204-44947474	GM12878	blood:	n/a	n/a
24	BATF	chr6:44977334-44977648	GM12878	blood:	n/a	chr6:44977540-44977551
25	BCL3	chr6:44934546-44934913	K562	blood:	n/a	n/a
26	BHLHE40	chr6:44891304-44891474	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:44928669-44928955	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:45016926-45017297	K562	blood:	n/a	n/a
29	BHLHE40	chr6:44969459-44969727	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:44934500-44934832	K562	blood:	n/a	n/a
31	BRCA1	chr6:45011813-45011861	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr6:44934371-44934913	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:44940388-44940854	K562	blood:	n/a	n/a
34	CBX3	chr6:44934407-44934915	K562	blood:	n/a	n/a
35	CBX3	chr6:44940439-44940814	K562	blood:	n/a	n/a
36	CBX3	chr6:44934427-44934905	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:44934470-44934850	K562	blood:	n/a	n/a
38	CBX3	chr6:45016920-45017304	K562	blood:	n/a	n/a
39	CBX3	chr6:44928552-44929041	HCT-116	colon:	n/a	n/a
40	CCNT2	chr6:44934499-44934885	K562	blood:	n/a	n/a
41	CCNT2	chr6:44893177-44893452	K562	blood:	n/a	n/a
42	CCNT2	chr6:45003117-45003383	K562	blood:	n/a	n/a
43	CEBPB	chr6:44993927-44994118	HepG2	liver:	n/a	chr6:44994071-44994082 chr6:44994071-44994080 chr6:44994069-44994082 chr6:44994069-44994080 chr6:44994069-44994082
44	CEBPB	chr6:44971301-44971464	A549	lung:	n/a	n/a
45	CEBPB	chr6:44949010-44949210	HepG2	liver:	n/a	chr6:44949038-44949049
46	CEBPB	chr6:45000179-45000543	IMR90	lung:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
47	CEBPB	chr6:44934515-44934884	K562	blood:	n/a	chr6:44934624-44934633
48	CEBPB	chr6:45000170-45000547	HepG2	liver:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
49	CEBPB	chr6:45074584-45074778	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:44934459-44934809	A549	lung:	n/a	chr6:44934624-44934633

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45079679-45079729	SK-N-SH_RA	brain:	n/a
2	chr6:45079679-45079729	HMEC	breast:	n/a
3	chr6:45030454-45030504	AG09309	skin:	n/a
4	chr6:45030454-45030504	SKMC	muscle:	n/a
5	chr6:45030454-45030504	HEK293	kidney:	embryo
6	chr6:45079679-45079729	BJ	skin:	n/a
7	chr6:45030454-45030504	HRPEpiC	eye:	n/a
8	chr6:45079679-45079729	LNCaP	prostate:	n/a
9	chr6:45079679-45079729	MCF-7	breast:	n/a
10	chr6:45030454-45030504	HCF	heart:	n/a
11	chr6:45030454-45030504	SAEC	small airway:	n/a
12	chr6:45079679-45079729	AG09319	gingival:	n/a
13	chr6:45079679-45079729	CMK	blood:	n/a
14	chr6:45079679-45079729	AoSMC	blood vessel:	n/a
15	chr6:45079679-45079729	HEK293	kidney:	embryo
16	chr6:45030454-45030504	HAEpiC	amniotic membrane:	n/a
17	chr6:45030454-45030504	H1-hESC	embryonic stem cell:	embryo
18	chr6:45030454-45030504	CMK	blood:	n/a
19	chr6:45079679-45079729	IMR90	lung:	fetal
20	chr6:45079679-45079729	HCT-116	colon:	n/a
21	chr6:45079679-45079729	U87	brain:	n/a
22	chr6:45030454-45030504	AG04449	skin:	fetal
23	chr6:45079679-45079729	NHDF-neo	bronchial:	n/a
24	chr6:45030454-45030504	HNPCEpiC	eye:	n/a
25	chr6:45030454-45030504	HCPEpiC	choroid plexus:	n/a
26	chr6:45030454-45030504	GM06990	blood:	n/a
27	chr6:45079679-45079729	Jurkat	blood:	n/a
28	chr6:45079679-45079729	ECC-1	luminal epithelium:	n/a
29	chr6:45030454-45030504	GM12891	blood:	n/a
30	chr6:45079679-45079729	H1-hESC	embryonic stem cell:	embryo
31	chr6:45030454-45030504	BJ	skin:	n/a
32	chr6:45079679-45079729	HNPCEpiC	eye:	n/a
33	chr6:45079679-45079729	PFSK-1	brain:	n/a
34	chr6:45030454-45030504	RPTEC	kidney:	n/a
35	chr6:45079679-45079729	PANC-1	pancreas:	n/a
36	chr6:45030454-45030504	K562	blood:	n/a
37	chr6:45030454-45030504	GM12892	blood:	n/a
38	chr6:45030454-45030504	ProgFib	skin:	n/a
39	chr6:45030454-45030504	Jurkat	blood:	n/a
40	chr6:45079679-45079729	Hepatocyte	liver:	n/a
41	chr6:45079679-45079729	AG10803	skin:	n/a
42	chr6:45030454-45030504	ovcar-3	ovarian:	n/a
43	chr6:45079679-45079729	GM12892	blood:	n/a
44	chr6:45079679-45079729	HRPEpiC	eye:	n/a
45	chr6:45030454-45030504	AG04450	lung:	fetal
46	chr6:45030454-45030504	HIPEpiC	eye:	n/a
47	chr6:45030454-45030504	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:45079679-45079729	RPTEC	kidney:	n/a
49	chr6:45079679-45079729	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:45030454-45030504	HRCEpiC	kidney:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
2	chr6:45054176..45055264-chr6:45386958..45387535,3	MCF-7	breast:
3	chr6:44928658..44930221-chr6:45326668..45328264,2	K562	blood:
4	chr6:44443174..44444085-chr6:45053756..45054587,2	MCF-7	breast:
5	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
6	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
7	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
8	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
9	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
10	chr6:45061664..45064501-chr6:45066770..45068668,2	K562	blood:
11	chr12:48357281..48357866-chr6:45012051..45012551,2	Hela-S3	cervix:
12	chr6:45083331..45086142-chr6:45155794..45158780,2	K562	blood:
13	chr6:45061664..45064501-chr6:45066770..45068668,2	K562	blood:
14	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:
15	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
16	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
17	chr6:44888776..44891351-chr6:45344894..45347692,2	K562	blood:
18	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
19	chr6:44996729..44999425-chr6:45119837..45121459,2	K562	blood:
20	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
21	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:
22	chr6:45049112..45051418-chr6:45052257..45055062,3	K562	blood:
23	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
24	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:
25	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
26	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
27	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
28	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
29	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:
30	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
31	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
32	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:
33	chr6:45049112..45051418-chr6:45052257..45055062,3	K562	blood:
34	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
35	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:
36	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
37	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
38	chr6:45054220..45054815-chr6:45386791..45387562,3	MCF-7	breast:
39	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
40	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
41	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
42	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
43	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:

No data

Variant related genes	Relation type
SUPT3H	TF binding region
SUPT3H	CpG island
ENSG00000134291	chromatin interactions
ENSG00000196284	chromatin interactions

Extended variants
information (count: 6686 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:6686 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs508494	chr6:44890760-44890761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548375972	chr6:44890803-44890804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566884549	chr6:44890806-44890807	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182833429	chr6:44890825-44890826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs638812	chr6:44890828-44890829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552510039	chr6:44890867-44890868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs510167	chr6:44890884-44890885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs538103428	chr6:44890886-44890887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370858155	chr6:44890889-44890890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556387887	chr6:44890950-44890951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148772061	chr6:44891033-44891034	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536382504	chr6:44891063-44891064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369397063	chr6:44891133-44891134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572869769	chr6:44891210-44891211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539867153	chr6:44891211-44891212	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs3799983	chr6:44891262-44891263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577255002	chr6:44891375-44891376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544507523	chr6:44891476-44891477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112870770	chr6:44891542-44891543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs669087	chr6:44891585-44891586	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs559852046	chr6:44891665-44891666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541978484	chr6:44891714-44891715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560397379	chr6:44891749-44891750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114607528	chr6:44891751-44891752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552291930	chr6:44891770-44891771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187477943	chr6:44891781-44891782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531922568	chr6:44891843-44891844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376309008	chr6:44891844-44891845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144268243	chr6:44891914-44891915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568345125	chr6:44891983-44891984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535694467	chr6:44891986-44891987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554311225	chr6:44892010-44892011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201312747	chr6:44892012-44892013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146560391	chr6:44892026-44892027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533879699	chr6:44892121-44892122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536023480	chr6:44892130-44892131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114320821	chr6:44892134-44892135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191983847	chr6:44892154-44892155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140929408	chr6:44892263-44892264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150378086	chr6:44892335-44892336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574640883	chr6:44892362-44892363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545848490	chr6:44892364-44892365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560246660	chr6:44892398-44892399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572495172	chr6:44892407-44892408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546271000	chr6:44892408-44892409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548544983	chr6:44892459-44892460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563366870	chr6:44892528-44892529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531577901	chr6:44892600-44892601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549738796	chr6:44892621-44892622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184556593	chr6:44892676-44892677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44877800-44892800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr6:44881000-44894600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:44885600-44899200	Weak transcription	Fetal Stomach	stomach
4	chr6:44887000-44893200	Weak transcription	NHDF-Ad	bronchial
5	chr6:44888000-44893000	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr6:44888000-44893800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr6:44888000-44896200	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr6:44888200-44896200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:44888400-44893800	Enhancers	Primary T cells from cord blood	blood
10	chr6:44888600-44893600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr6:44889200-44890800	Enhancers	Liver	Liver
12	chr6:44889200-44891000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:44889200-44891200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr6:44889200-44891400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:44889200-44892800	Weak transcription	K562	blood
16	chr6:44889200-44893000	Weak transcription	NH-A	brain
17	chr6:44889400-44892800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:44889600-44892800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr6:44890000-44891400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr6:44890000-44892800	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr6:44890000-44893000	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr6:44890000-44893000	Weak transcription	Stomach Mucosa	stomach
23	chr6:44890200-44892800	Weak transcription	Fetal Heart	heart
24	chr6:44890200-44893000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr6:44890600-44892800	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr6:44890600-44893000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:44891000-44893800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:44891200-44891800	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr6:44891200-44891800	Enhancers	Dnd41	blood
30	chr6:44891400-44891600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr6:44891400-44891600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr6:44891400-44893800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr6:44891600-44892000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:44891800-44892800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr6:44891800-44893000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr6:44891800-44898400	Weak transcription	Dnd41	blood
37	chr6:44892000-44892800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:44892800-44893000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:44892800-44893000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr6:44892800-44893200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:44892800-44893200	Enhancers	Primary T cells fromperipheralblood	blood
42	chr6:44892800-44893200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr6:44892800-44893200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr6:44892800-44893200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:44892800-44893600	Enhancers	Primary hematopoietic stem cells	blood
46	chr6:44892800-44893600	Enhancers	Fetal Heart	heart
47	chr6:44892800-44893600	Enhancers	K562	blood
48	chr6:44893000-44893200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr6:44893000-44893200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:44893000-44893200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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